Structure Information
Structure

Compound Identification

SMILES

NC(=O)C1=C(NC(=O)COC(=O)CCN2C(=O)C3=C(C2=O)C(=CC=C3)[N+]([O-])=O)SC=C1

InChIKey

InChIKey=RYHCMRKORSBZMC-UHFFFAOYSA-N

Formula

C18H14N4O8S

Mass

446.39

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic acids and derivatives

Class

Peptidomimetics

Subclass

Depsipeptides

Intermediate Tree Nodes

Not available

Direct Parent

Depsipeptides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Depsipeptide - Indolyl carboxylic acid derivative - Phthalimide - Isoindolone - Indole - Isoindoline - Isoindole - Isoindole or derivatives - Nitroaromatic compound - Thiophene carboxamide - Thiophene carboxylic acid or derivatives - N-arylamide - Benzenoid - Carboxylic acid imide, n-substituted - Vinylogous amide - Carboxylic acid imide - Heteroaromatic compound - Thiophene - Organic nitro compound - Carboxylic acid ester - C-nitro compound - Primary carboxylic acid amide - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - Azacycle - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organic oxoazanium - Organopnictogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organooxygen compound - Organic zwitterion - Organic nitrogen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids), commonly but not necessarily regularly alternating.

External Descriptors

Not available

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